WO2001048080A1 - Thermoplastic olefin nanocomposite - Google Patents

Thermoplastic olefin nanocomposite Download PDF

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Publication number
WO2001048080A1
WO2001048080A1 PCT/US2000/034707 US0034707W WO0148080A1 WO 2001048080 A1 WO2001048080 A1 WO 2001048080A1 US 0034707 W US0034707 W US 0034707W WO 0148080 A1 WO0148080 A1 WO 0148080A1
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WO
WIPO (PCT)
Prior art keywords
composition
maleated polypropylene
maleated
average molecular
polymer
Prior art date
Application number
PCT/US2000/034707
Other languages
English (en)
French (fr)
Inventor
Chai-Jing Chou
Eddy I. Garcia-Meitin
Lonnie Schilhab
Richard F. Fibiger
Original Assignee
The Dow Chemical Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US10/169,483 priority Critical patent/US7084199B1/en
Application filed by The Dow Chemical Company filed Critical The Dow Chemical Company
Priority to KR1020027008452A priority patent/KR20020062997A/ko
Priority to DE60016046T priority patent/DE60016046T2/de
Priority to AT00986634T priority patent/ATE296332T1/de
Priority to MXPA02006567A priority patent/MXPA02006567A/es
Priority to BR0016948-0A priority patent/BR0016948A/pt
Priority to CA002395782A priority patent/CA2395782A1/en
Priority to JP2001548611A priority patent/JP2003518542A/ja
Priority to EP00986634A priority patent/EP1268656B1/en
Publication of WO2001048080A1 publication Critical patent/WO2001048080A1/en

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F255/00Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
    • C08F255/02Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/14Copolymers of propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/26Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/006Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to block copolymers containing at least one sequence of polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/06Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

Definitions

  • thermoplastic polyolefin incorporating polypropylene reinforced with delaminated or exfoliated cation-exchanging multi- layered silicates.
  • the first approach (also described by Kawasumi et al . ) was to blend a quaternary ammonium exchanged multi-layered silicate with a maleic anhydride modified polypropylene oligomer and then add an unmodified polypropylene polymer.
  • the maleic anhydride modified polypropylene oligomer had sufficient polarity to exfoliate the silicate under the shear conditions of the blending process.
  • the second approach of Usuki et al . was to blend a quaternary ammonium exchanged multi-layered silicate with a maleic anhydride modified polypropylene polymer.
  • the maleic anhydride modified polypropylene polymer had sufficient polarity to exfoliate the silicate under the shear conditions of the blending process.
  • Usuki et al . pointed out that when a maleic anhydride modified polypropylene oligmer was not used, then the average molecular weight of the maleic anhydride modified polypropylene polymer should be limited to about 100,000.
  • Thermoplastic olefin is a mechanical blend of a polyolefin (such as polypropylene) and a thermoplastic elastomer (such as EPDM or ultra low density polyethylene) .
  • a polyolefin such as polypropylene
  • a thermoplastic elastomer such as EPDM or ultra low density polyethylene
  • the instant invention provides a polypropylene based TPO nanocomposite with a significantly increased low temperature impact toughness.
  • the key to achieving such toughness is the use of maleated polypropylene polymer having a molecular weight greater than 100,000.
  • the instant invention is a thermoplastic olefin nanocomposite composition, comprising: a maleated polypropylene polymer phase having a weight average molecular weight greater than 100,000; a cation exchanging layered silicate material dispersed in the maleated polypropylene phase so that more than one half of the cation exchanging layered silicate material is present as one, two, three, four or five layer units upon examination by electron microscopy; and a thermoplastic elastomer phase interdispersed with the maleated polypropylene phase.
  • the instant invention is a polypropylene nanocomposite composition, comprising: a maleated polypropylene polymer having a weight average molecular weight greater than 100,000; and a cation exchanging layered silicate material dispersed in the maleated polypropylene phase so that more than one half of the cation exchanging layered silicate material is present as one, two, three, four or five layer units upon examination by electron microscopy.
  • An article of manufacture comprising an object formed of a composition comprising: a maleated polypropylene polymer phase having a weight average molecular weight greater than 100,000; a cation exchanging layered silicate material dispersed in the maleated polypropylene phase so that more than one half of the cation exchanging layered silicate material is present as one, two, three, four or five layer units upon examination by electron microscopy; and a thermoplastic elastomer phase interdispersed with the maleated polypropylene phase.
  • An article of manufacture comprising an object formed of a composition comprising: a maleated polypropylene polymer having a weight average molecular weight greater than 100,000; and a cation exchanging layered silicate material dispersed in the maleated polypropylene so that more than one half of the cation exchanging layered silicate material is present as one, two, three, four or five layer units upon examination by electron microscopy.
  • thermoplastic olefin nanocomposite composition comprising the steps of: mixing a softened or melted polypropylene polymer with an organic peroxide and maleic anhydride to form a maleated polypropylene polymer; mixing the maleated polypropylene polymer with an onium treated cation exchanging layered silicate material to form a maleated polypropylene nanocomposite; and mixing the maleated polypropylene nancomposiite with a thermoplastic elastomer, the process characterized by the maleated polypropylene having a weight average molecular weight greater than 100,000.
  • a process for producing a polypropylene nanocomposite composition comprising the steps of: mixing a softened or melted polypropylene polymer with an organic peroxide and maleic anhydride to form a maleated polypropylene polymer; and mixing the maleated polypropylene polymer with an onium treated cation exchanging layered silicate material to form a maleated polypropylene nanocomposite, the process characterized by the maleated polypropylene having a weight average molecular weight greater than 100,000.
  • Fig. 1 is an idealized drawing made from an electron photomicrographic examination of the maleated polypropylene phase of a TPO composition of the instant invention showing more than one half of the cation exchanging layered silicate material being present as one, two, three, four or five layer units.
  • thermoplastic olefin (TPO) nanocomposite of the instant invention comprises a maleated polypropylene polymer phase having a weight average molecular weight greater than 100,000, a cation exchanging layered silicate material dispersed in the maleated polypropylene so that more than one half of the cation exchanging layered silicate material is present as one, two, three, four or five layer units upon examination by electron microscopy (and most preferably, more than one half of the material is so apparent as one, two or three layer units) and a thermoplastic elastomer phase interdispersed with the maleated polypropylene phase.
  • the weight average molecular weight of the maleated polypropylene polymer can be significantly greater than 100,000, for example, it can be greater than 150,000 or even greater than 250, 000.
  • Fig. 1 therein is shown a drawing reproduction of an electron photomicrograph of the maleated polypropylene polymer phase of a TPO composition of the instant invention.
  • the layered silicate material is shown delaminated or exfoliated as: three single layer units, one two layer unit, one three layer unit, one four layer unit, one five layer unit and two eight layer units.
  • a one layer unit typically is a platlet about 1-10 nanometers thick and 100-1000 nanometers wide.
  • weight average molecular weight is well known in the instant art and can be determined by, for example, gel permeation chromatography .
  • cation exchanging layered silicate material is well known in the instant art and includes the "clay mineral” of United States Patent 5,973,053, fully incorporated herein by reference. Examples of cation exchanging layered silicate materials include:
  • Zeolitic layered materials such as ITQ-2, MCM- 22 precursor, exfoliated ferrierite and exfoliated mordenite.
  • any of the naturally occurring or synthetic cation exchanging layered silicate clay materials may be used in the present invention.
  • Preferred are smectite clays, including montmorillonite, bidelite, saponite and hectorite.
  • an "onium treated cation exchanging layered silicate material” is a cation exchanging layered silicate material that has been exposed to onium cations (usually oranic quaternary ammonium compounds) so that the original cation of the cation exchanging layered silicate material is exchanged, at least in part, for the onium cations.
  • Onium treated cation exchanging layered silicate materials are well known in the instant art, for example, see the above mentioned United States Patent 5,973,053. Onium treated cation exchanging layered silicate materials are commercially available from, for example, Southern Clay Company in the United States.
  • the term "maleated polypropylene" means a polypropylene containing more than one tenth of one percent of maleic anhydride grafted to the polypropylene. Maleated polypropylene is commercially available from several sources. Polymer synthesis may be the best way to tailor the molecular weight, molecular weight distribution and the extent of maleic anhydride grafting to the polymer.
  • maleated polypropylene can be made by mixing softened or melted unmodified polypropylene with maleic anhydride and an organic peroxide.
  • the weight percent of maleic anhydride of the maleated polypropylene is in the range of from two tenths of one percent to ten percent. Most preferably, the weight percent of maleic anhydride of the maleated polypropylene is in the range of from one half of one percent to two percent.
  • the amount of cation exchanging layered silicate material used can range from one to fifty percent by weight of the composition. Preferably, the amount of cation exchanging layered silicate material used ranges from three to twelve percent by weight of the composition.
  • the polypropylene nanocomposite composition of the instant invention is obtained when the above discussed thermoplastic elastomer is not used.
  • the TPO nanocomposite or polyropylene nanocomposite of the instant invention can also contain conventional macro sized fillers such as a carbonate, glass fibers, kaolin, talc, glass beads, graphite fibers and carbon black.
  • the maleated polypropylene of the instant invention can be high crystallinity maleated polypropylene.
  • the term "high crystallinity" is defined herein as material which has a heat of melting of the maleated polypropylene crystallites of more than 85 Joules per gram of amorphous and crystalline phases of the polymer using the determination outlined on pages 448-494 of Volume 4 of the Encyclopedia of Polymer Science and Engineering, 2 nd Edition, 1986, John Wiley & Sons.
  • the TPO nanocomposite or polypropylene nanocomposite of the instant invention can also comprise non-maleated polypropylene having a weight average molecular weight greater than 100,000.
  • the TPO nanocomposite or polypropylene nanocomposite of the instant invention is essentially free of maleated polypropylene oligomer, that is, the concentration of maleated polypropylene oligomer is less than five percent of the total amount of polypropylene.
  • oligomer herein means a polymer having a molecular weight of less than one thousand.
  • the non-maleated polypropylene can be any type of polypropylene, for example, block co-polymers of polypropylene and ethylene .
  • the TPO nanocomposite of the instant invention can be made by mixing a heat softened or melted polypropylene polymer of sufficiently high molecular weight with an organic peroxide and maleic anhydride to form a maleated polypropylene polymer which can then mixed with an onium treated cation exchanging layered silicate material and a thermoplastic elastomer.
  • Another way of making the TPO nanocomposite of the instant invention is to mix a heat softened or melted polypropylene polymer of sufficiently high molecular weight with an organic peroxide and maleic anhydride to form a maleated polypropylene polymer, then mix the maleated polypropylene polymer with an onium treated cation exchanging layered silicate material and then to mix in the thermoplastic elastomer.
  • the polypropylene nanocomposite of the instant invention can be made by mixing a heat softened or melted polypropylene polymer of sufficiently high molecular weight with an organic peroxide and maleic anhydride to form a maleated polypropylene polymer which can then mixed w th an onium treated cation exchanging layered silicate material.
  • the TPO nanocomposite or polypropylene nanocomposite of the instant invention can be used, for example, to make articles of manufacture such as parts for motor vehicles, appliances, business machines or construction articles.
  • maleated polypropylene having a weight average molecular weight of 150,000 (laboratory prepared by mixing ninety five parts high molecular weight polypropylene with three parts of maleic anhydride and six tenths part di-cumyl peroxide in a BANBURY brand polymer mixer at 200 rpm and 180-200 degrees Celsius for three minutes), thirty three parts by weight of thermoplastic elastomer (AFFINITY 8180 brand low density polyethylene from Dow) and ten parts by weight onium treated cation exchanging layered silicate material (montmorillonite treated with dimethyl, dihydrogenated tallow quaternary ammonium compound from Southern Clay) are mixed in a BANBURY brand polymer mixer at 100 rpm and a temperature of 150 degrees Celsius for ten minutes to produce a thermoplastic olefin nanocomposite having a flex modulus of 183,000 pounds per square inch and a notched IZOD impact strength at 30 degrees below zero Centigrade of 11.6 foot pound per
  • thermoplastic elastomer AFFINITY 8180 brand low density polyethylene from Dow
  • onium treated cation exchanging layered silicate material montmorillonite treated with dimethyl, dihydrogenated tallow quaternary ammonium compound from Southern Clay
  • thermoplastic elastomer AFFINITY 8180 brand low density polyethylene from Dow
  • onium treated cation exchanging layered silicate material montmorillonite treated with dimethyl, dihydrogenated tallow quaternary ammonium compound from Southern Clay
  • thermoplastic elastomer AFFINITY 8180 brand low density polyethylene from Dow
  • talc ten parts by weight onium treated cation exchanging layered silicate material (montmorillonite treated with dimethyl, dihydrogenated tallow quaternary ammonium compound from Southern Clay)
  • onium treated cation exchanging layered silicate material montmorillonite treated with dimethyl, dihydrogenated tallow quaternary ammonium compound from Southern Clay
  • EXAMPLE 5 Ninety parts by weight of maleated polypropylene having a weight average molecular weight of 200,000, ten parts by weight of onium treated cation exchanging layered silicate material (montmorillonite treated with dimethyl, dihydrogenated tallow quaternary ammonium compound from Southern Clay) and two tenths part by weight of IRGONOX
  • B225 brand antioxidant are mixed in a HAAKE brand polymer mixer at 200 rpm and a temperature of 180 degrees Celsius for ten minutes to produce a polypropylene nanocomposite. Electron microscopy examination of the polypropylene nanocomposite shows that more than one half of the onium treated cation exchanging layered silicate material is present as single, double or triple layer units.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
PCT/US2000/034707 1999-12-29 2000-12-20 Thermoplastic olefin nanocomposite WO2001048080A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US10/169,483 US7084199B1 (en) 1999-12-29 1999-12-29 Thermoplastic olefin nanocomposite
KR1020027008452A KR20020062997A (ko) 1999-12-29 2000-12-20 열가소성 올레핀 나노합성물
DE60016046T DE60016046T2 (de) 1999-12-29 2000-12-20 Thermoplastisches nanokomposit auf basis von polypropylen und dessen herstellung
AT00986634T ATE296332T1 (de) 1999-12-29 2000-12-20 Thermoplastisches nanokomposit auf basis von polypropylen und dessen herstellung
MXPA02006567A MXPA02006567A (es) 1999-12-29 2000-12-20 Nanocompuesto de olefina termoplastica.
BR0016948-0A BR0016948A (pt) 1999-12-29 2000-12-20 Composições de nanocompósitos de olefina termoplástica e de polipropileno, processos para produzì-las e artigos de manufatura compreendendo objetos formados de tais composições
CA002395782A CA2395782A1 (en) 1999-12-29 2000-12-20 Thermoplastic olefin nanocomposite
JP2001548611A JP2003518542A (ja) 1999-12-29 2000-12-20 熱可塑性オレフィンナノ複合体
EP00986634A EP1268656B1 (en) 1999-12-29 2000-12-20 Thermoplastic olefin nanocomposite based on polypropylene and process for production thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US17360899P 1999-12-29 1999-12-29
US60/173,608 1999-12-29

Publications (1)

Publication Number Publication Date
WO2001048080A1 true WO2001048080A1 (en) 2001-07-05

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PCT/US2000/034707 WO2001048080A1 (en) 1999-12-29 2000-12-20 Thermoplastic olefin nanocomposite

Country Status (12)

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EP (1) EP1268656B1 (zh)
JP (1) JP2003518542A (zh)
KR (1) KR20020062997A (zh)
CN (1) CN1187406C (zh)
AT (1) ATE296332T1 (zh)
BR (1) BR0016948A (zh)
CA (1) CA2395782A1 (zh)
DE (1) DE60016046T2 (zh)
ES (1) ES2231297T3 (zh)
MX (1) MXPA02006567A (zh)
TW (1) TW593502B (zh)
WO (1) WO2001048080A1 (zh)

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WO2001096467A2 (en) * 2000-06-16 2001-12-20 Basell Technology Company B.V. Composite materials comprising propylene graft copolymers
WO2003022917A1 (en) * 2001-09-06 2003-03-20 Equistar Chemicals, Lp Propylene polymer compositions having improved melt strength
WO2004062896A1 (en) * 2003-01-16 2004-07-29 Ian Orde Michael Jacobs Methods, compositions and blends for forming articles having improved environmental stress crack resistance
US6770697B2 (en) 2001-02-20 2004-08-03 Solvay Engineered Polymers High melt-strength polyolefin composites and methods for making and using same
KR100443269B1 (ko) * 2001-04-12 2004-08-04 한국화학연구원 난연성 폴리올레핀계 수지 조성물
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US7037970B2 (en) 2001-12-20 2006-05-02 Equistar Chemicals, Lp Process for increasing the melt strength of ethylene-vinyl carboxylate copolymers
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US7288585B2 (en) 2003-06-24 2007-10-30 Ciba Specialty Chemicals Corp. Acrylic dispersing agents in nanocomposites
US7517353B2 (en) 2001-09-28 2009-04-14 Boston Scientific Scimed, Inc. Medical devices comprising nanomaterials and therapeutic methods utilizing the same
US7737211B2 (en) 2005-09-07 2010-06-15 Gm Global Technology Operations, Inc. Method for forming nanocomposite materials
US7837899B2 (en) 2003-03-03 2010-11-23 Polymers Australia Pty. Ltd. Dispersing agents in nanocomposites
US8012540B2 (en) 2006-04-07 2011-09-06 Addcomp Holland Bv Aqueous emulsion comprising a functionalized polyolefin and carbon nanotubes
US8039526B2 (en) 2006-04-05 2011-10-18 Exxonmobil Chemical Patents Inc. Thermoplastic vulcanizates including nanoclays and processes for making the same
US8080613B2 (en) 2002-11-08 2011-12-20 Advanced Polymerik Pty Ltd Process for the preparation of polyolefin nanocamposites
US8110626B2 (en) 2005-09-27 2012-02-07 Advanced Polymerik PTY. Limited Dispersing agents in composites
AU2012206982B2 (en) * 2003-01-16 2013-12-05 Viva Healthcare Packaging Limited Methods, compositions and blends for forming articles having improved environmental stress crack resistance

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JP4728544B2 (ja) * 2001-09-27 2011-07-20 積水化学工業株式会社 樹脂組成物の製造方法
JP4619780B2 (ja) * 2002-07-05 2011-01-26 エクソンモービル・ケミカル・パテンツ・インク 官能化されたエラストマーナノ複合物
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JP4943153B2 (ja) * 2003-06-12 2012-05-30 ダウ グローバル テクノロジーズ エルエルシー 難燃性組成物
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ATE296332T1 (de) 2005-06-15
DE60016046D1 (de) 2004-12-23
KR20020062997A (ko) 2002-07-31
CA2395782A1 (en) 2001-07-05
ES2231297T3 (es) 2005-11-16
EP1268656A1 (en) 2003-01-02
DE60016046T2 (de) 2006-03-02
MXPA02006567A (es) 2002-11-29
CN1413232A (zh) 2003-04-23
EP1268656B1 (en) 2005-05-25
JP2003518542A (ja) 2003-06-10
TW593502B (en) 2004-06-21
BR0016948A (pt) 2002-09-10

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